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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1440725Generated: November 2, 2026

Pyridine → 2-(Acetyloxy)-3,5-dichlorobenzenesulfonyl chloride

https://huagongshe.com/reaction/1440725

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetyl chlorideHCID 6367—
ReactantSulfuryl chlorideHCID 24648—
Reactant3,5-Dichloro-2-hydroxybenzenesulphonyl chlorideHCID 90078—
SolventDichloromethaneHCID 6344—
Product2-(Acetyloxy)-3,5-dichlorobenzenesulfonyl chlorideHCID 18981627—

Reaction Steps

A pyridine solution (1.1 g of pyridine in 10 ml of methylene chloride) was added dropwise over 30 minutes to a solution of 3.37 g of 3,5-dichloro-2-hydroxybenzenesulfonyl chloride, 25 ml of methylene chloride and 1.1 g of acetyl chloride. After two hours of stirring at room temperature the starting sulfonyl chloride was no longer present and one major product had formed. The reaction was concentrated and used immediately.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05500405
Source datasetuspto-grants-1996_03
ORD IDord-ea5f4a321882475a85378c65cc583a99
Source noteuspto-grants-1996_03